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表达针对病毒复制起始基因的小干扰 RNA 的转基因香蕉植物对感染香蕉束顶病毒表现出高水平的抗性。

Transgenic banana plants expressing small interfering RNAs targeted against viral replication initiation gene display high-level resistance to banana bunchy top virus infection.

机构信息

Nuclear Agriculture and Biotechnology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, India.

出版信息

J Gen Virol. 2012 Aug;93(Pt 8):1804-1813. doi: 10.1099/vir.0.041871-0. Epub 2012 May 2.

Abstract

The banana aphid-transmitted Banana bunchy top virus (BBTV) is the most destructive viral pathogen of bananas and plantains worldwide. Lack of natural sources of resistance to BBTV has necessitated the exploitation of proven transgenic technologies for obtaining BBTV-resistant banana cultivars. In this study, we have explored the concept of using intron-hairpin-RNA (ihpRNA) transcripts corresponding to viral master replication initiation protein (Rep) to generate BBTV-resistant transgenic banana plants. Two ihpRNA constructs namely ihpRNA-Rep and ihpRNA-ProRep generated using Rep full coding sequence or Rep partial coding sequence together with its 5' upstream regulatory region, respectively, and castor bean catalase intron were successfully transformed into banana embryogenic cells. ihpRNA-Rep- and ihpRNA-ProRep-derived transgenic banana plants, selected based on preliminary screening for efficient reporter gene expression, were completely resistant to BBTV infection as indicated by the absence of disease symptoms after 6 months of viruliferous aphid inoculation. The resistance to BBTV infection was also evident by the inability to detect cDNAs coding for viral coat protein, movement protein and Rep protein by RT-PCR from inoculated transgenic leaf extracts. Southern analysis of the two groups of transgenics showed that ihpRNA transgene was stably integrated into the banana genome. The detection of small interfering RNAs (siRNAs) derived from the ihpRNA transgene sequence in transformed BBTV-resistant plants positively established RNA interference as the mechanism underlying the observed resistance to BBTV. Efficient screening of optimal transformants in this vegetatively propagated non-segregating fruit crop ensured that all the transgenic plants assayed were resistant to BBTV infection.

摘要

香蕉束顶病毒(BBTV)是世界范围内香蕉和大蕉最具破坏性的病毒病原体。缺乏对 BBTV 的天然抗性来源,使得利用已证明的转基因技术获得 BBTV 抗性的香蕉品种成为必要。在这项研究中,我们探索了使用对应病毒主复制起始蛋白(Rep)的内含子发夹 RNA(ihpRNA)转录本产生 BBTV 抗性转基因香蕉植物的概念。我们成功地将两个 ihpRNA 构建体,即 ihpRNA-Rep 和 ihpRNA-ProRep,转化到香蕉胚性细胞中,这两个构建体分别使用 Rep 的全长编码序列或 Rep 的部分编码序列及其 5'上游调控区,与蓖麻过氧化氢酶内含子一起构建。基于对有效报告基因表达的初步筛选,选择了 ihpRNA-Rep 和 ihpRNA-ProRep 衍生的转基因香蕉植物,在接种毒蚜虫 6 个月后,由于没有出现疾病症状,表明它们完全抵抗 BBTV 感染。从接种的转基因叶片提取物中通过 RT-PCR 无法检测到编码病毒外壳蛋白、运动蛋白和 Rep 蛋白的 cDNA,也表明了对 BBTV 感染的抗性。对两组转基因植物的 Southern 分析表明,ihpRNA 转基因稳定整合到香蕉基因组中。在转化的 BBTV 抗性植物中检测到源自 ihpRNA 转基因序列的小干扰 RNA(siRNA),这一结果正向证明了 RNA 干扰是观察到的对 BBTV 抗性的机制。在这种无性繁殖的非分离水果作物中,对最佳转化体的有效筛选确保了所有检测到的转基因植物都对 BBTV 感染具有抗性。

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